Publication:
Revisiting TOP2B-related phenotypes: three new cases and literature review

dc.contributor.coauthorKalayci, Tugba
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.departmentGraduate School of Health Sciences
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorÇepni, Ece
dc.contributor.kuauthorBörklü Yücel, Esra
dc.contributor.kuauthorAvcı, Şahin
dc.contributor.kuauthorEraslan, Serpil
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF HEALTH SCIENCES
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:29:49Z
dc.date.issued2023
dc.description.abstractDNA Topoisomerase II beta (TOP2B) acts on DNA topology during transcription and has a critical role in neural development. Heterozygous pathogenic changes in its encoding gene, TOP2B (MIM *126431), has been linked with three overlapping phenotypes characterized by immunodeficiency, acral and urogenital anomalies: Hoffman, BILU and Ablepharon-macrostomia-like syndrome. We herein report on a mother and two sons with distinct TOP2B-phenotype. Two males reported further delineated genital phenotype of males and all reported patients were reviewed for genotypephenotype correlation. We believe the patients reported herein along with the previously defined 11 represent a phenotypic spectrum from mild-to-severe immunological, acral and urogenital involvement, for which we propose the acronym "TOP2B-related Immunodeficiency and Congenital Anomalies Spectrum (TICAS)".
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue2
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipTUBITAK, grant number 112S398 (E-RARE network CRANIRARE2) to HK.
dc.description.volume104
dc.identifier.doi10.1111/cge.14341
dc.identifier.eissn1399-0004
dc.identifier.issn0009-9163
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85153229201
dc.identifier.urihttps://doi.org/10.1111/cge.14341
dc.identifier.urihttps://hdl.handle.net/20.500.14288/25954
dc.identifier.wos971729100001
dc.keywordsB-cell immunodeficiency
dc.keywordsBILU syndrome
dc.keywordsHoffman syndrome
dc.keywordsTOP2B gene
dc.language.isoeng
dc.publisherWiley
dc.relation.grantnoTUBITAK [112S398]
dc.relation.ispartofClinical Genetics
dc.subjectGenetics and heredity
dc.titleRevisiting TOP2B-related phenotypes: three new cases and literature review
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorÇepni, Ece
local.contributor.kuauthorBörklü Yücel, Esra
local.contributor.kuauthorAvcı, Şahin
local.contributor.kuauthorEraslan, Serpil
local.contributor.kuauthorKayserili, Hülya
local.publication.orgunit1GRADUATE SCHOOL OF HEALTH SCIENCES
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1KUH (KOÇ UNIVERSITY HOSPITAL)
local.publication.orgunit2KUH (Koç University Hospital)
local.publication.orgunit2School of Medicine
local.publication.orgunit2Graduate School of Health Sciences
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